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HRID 9717作成日:2026年10月24日

Acetonitrile → 10-methoxy-5H-dibenz(b,f)azepine-5-carboxamide

https://huagongshe.com/ja/reaction/9717

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物10-MethoxyiminostilbeneHCID 78424—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物HCID 178418852HCID 178418852—
溶媒WaterHCID 962—
生成物10-methoxy-5H-dibenz(b,f)azepine-5-carboxamideHCID 12003150.7%

反応手順

10-methoxy-5H-dibenz(b,f)azepine (29.9 g, 0.134 mol) was added to 300 ml acetonitrile in a three-neck flask (500 ml) equipped with a mechanical stirring apparatus. The mixture was stirred at room temperature for 15 minutes, and then NaOCN (18 g, 0.277 mol) was added, followed by pyridinium p-toluenesulfonate (75 g, 0.3 mol). The mixture was stirred at room temperature for about 4 hours, at which time TLC indicated that the reaction was complete (disappearance of 10-methoxy-5H-dibenz(b,f)azepine). 30 ml water was added, and the mixture stirred for 15 minutes. The solids were filtered and the filtrate was concentrated under vacuum. The semi-solid residue was triturated with acetone to provide a creamy solid, which was dried at 80° C. to provide 18 g (0.068 mol, 50% yield) of 10-methoxy-5H-dibenz[b,f]azepine-5-carboxamide (10-methoxycarbamazepine).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091339B2
出典データセットuspto-grants-2006_08
ORD IDord-ce0dd8900c0f4904b3ae6c61be0151bc
出典メモuspto-grants-2006_08